Literature DB >> 5771531

Hereditary renal-retinal dysplasia.

R N Schimke.   

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Year:  1969        PMID: 5771531     DOI: 10.7326/0003-4819-70-4-735

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


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  10 in total

1.  Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness.

Authors:  M P Clarke; T J Sullivan; C Francis; R Baumal; T Fenton; W G Pearce
Journal:  Br J Ophthalmol       Date:  1992-03       Impact factor: 4.638

2.  Neurological abnormalities in congenital amaurosis of Leber. Review of 30 cases.

Authors:  M J Vaizey; M D Sanders; K C Wybar; J Wilson
Journal:  Arch Dis Child       Date:  1977-05       Impact factor: 3.791

3.  A new syndrome with ocular, skeletal and renal involvement.

Authors:  M Cirillo Silengo; G Lopez Bell; M Biagioli; A Guala; G Porcellini; P Franceschini
Journal:  Pediatr Radiol       Date:  1987

4.  Nephronophthisis (medullary cystic disease).

Authors:  R N Srivastava; O P Ghai; R K Chandra
Journal:  Arch Dis Child       Date:  1971-06       Impact factor: 3.791

5.  The nephronophthisis complex. A clinicopathologic study in children.

Authors:  R Waldherr; T Lennert; H P Weber; H J Födisch; K Schärer
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1982

6.  Sector retinitis pigmentosa in juvenile nephronophthisis.

Authors:  V Godel; A Iaina; P Nemet; M Lazar
Journal:  Br J Ophthalmol       Date:  1980-02       Impact factor: 4.638

7.  Fundus changes in mesangiocapillary glomerulonephritis type II: clinical and fluorescein angiographic findings.

Authors:  J Duvall-Young; C D Short; M F Raines; R Gokal; W Lawler
Journal:  Br J Ophthalmol       Date:  1989-11       Impact factor: 4.638

8.  Familial juvenile nephronophthisis, Jeune's syndrome, and associated disorders.

Authors:  M D Donaldson; A A Warner; R S Trompeter; G B Haycock; C Chantler
Journal:  Arch Dis Child       Date:  1985-05       Impact factor: 3.791

9.  Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye.

Authors:  Katie Weihbrecht; Wesley A Goar; Thomas Pak; Janelle E Garrison; Adam P DeLuca; Edwin M Stone; Todd E Scheetz; Val C Sheffield
Journal:  Med Res Arch       Date:  2017-09-18

10.  Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome.

Authors:  Satoshi Katagiri; Takaaki Hayashi; Kazutoshi Yoshitake; Noriyuki Murai; Zenichi Matsui; Hiroyuki Kubo; Hiroyuki Satoh; Senya Matsufuji; Tsuyoshi Takamura; Takashi Yokoo; Yoshihiro Omori; Takahisa Furukawa; Takeshi Iwata; Tadashi Nakano
Journal:  Sci Rep       Date:  2018-11-13       Impact factor: 4.379

  10 in total

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